Jolca SA
FDA import alert and refusal historyHuevar De Aljarafe, SpainFEI 3004271256
Recorded by FDA as Jolca SA; Jolca, S.A.
As of October 26, 2026, Jolca SA has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on July 22, 2022, was classified VAI (Voluntary Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- Seafood HACCP/CGMP for Foods/Adulterated
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Jolca SA
3 records, newest first. Each line links to the FDA page it came from.
2024
- Warning letterWarning letter issuedSeafood HACCP/CGMP for Foods/AdulteratedSource
2022
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Jolca SA
- Is Jolca SA on an FDA import alert?
- No listing for Jolca SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
- Has FDA refused shipments from Jolca SA?
- No FDA import refusals for Jolca SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- Has Jolca SA received an FDA warning letter?
- Yes. FDA issued a warning letter to Jolca SA on March 21, 2024 (Seafood HACCP/CGMP for Foods/Adulterated).
- When was Jolca SA last inspected by FDA?
- FDA's most recent inspection of Jolca SA with a final classification is dated July 22, 2022 and was classified VAI (Voluntary Action Indicated).
- What is Jolca SA's FEI number?
- Jolca SA's FDA Establishment Identifier (FEI) is 3004271256.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.